4.5 Article

Sarcopenia is associated with disability status-results from the KORA-Age study

Journal

OSTEOPOROSIS INTERNATIONAL
Volume 28, Issue 7, Pages 2069-2079

Publisher

SPRINGER LONDON LTD
DOI: 10.1007/s00198-017-4027-y

Keywords

Disability; EWGSOP; Muscle mass; Older people; Sarcopenia

Funding

  1. German Research Foundation (Deutsche Forschungsgemeinschaft) [GR 3608/1-1]
  2. German Federal Ministry of Education and Research (BMBF) [FKZ 01ET0713, FKZ 01ET1003A, FKZ 01ET1003C]
  3. Kompetenznetz Adipositas (Competence Network Obesity) - German Federal Ministry of Education and Research [FKZ 01GI1121B]

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We estimated the prevalence of sarcopenia and its impact on disability in older people. Sarcopenia was found to contribute to higher disability scores. However, our study was not able to show any influence of sarcopenia on the rate of functional decline. This directs attention to an accurate diagnosis of sarcopenia as the onset may be influenced, but its rate may not. The objectives of this study using data from a population-based cohort were to estimate the prevalence of sarcopenia in older people in Germany and to test the hypothesis that sarcopenia is associated with disability in older adults. Cross-sectional (n = 927) and longitudinal analyses (n = 859) of participants aged ae65 years at baseline from southern Germany enrolled in the Cooperative Health Research in the Region Augsburg (KORA)-Age study (2009-2012). Sarcopenia was defined based on the European Working Group on Sarcopenia in Older People (EWGSOP) algorithm which includes the presence of both low muscle mass and low muscle function (strength or performance). Disability status was measured by the Health Assessment Questionnaire-Disability Index (HAQ-DI). The presence of disability was defined as HAQ-DI > 0. Directed acyclic graphs (DAGs) were constructed to identify potential confounders. The effect of sarcopenia on disability was analyzed using linear mixed effect models with disability values as a continuous outcome. The overall prevalence of sarcopenia was 5.7% (men 4.0%, women 7.5%) and increased with age. The 3-year incidence of disability was 32.7%. After adjustment for potential confounders, presence of sarcopenia was significantly associated with higher disability scores (0.142 [confidence interval 0.029-0.254]). The prevalence of sarcopenia is consistent with estimates from other European studies using this algorithm. Our results suggest that sarcopenia can contribute to higher disability scores in older adults. However, our study was not able to show any influence of sarcopenia on the rate of functional decline using the EWGSOP diagnostic algorithm for sarcopenia. This directs attention to an accurate diagnosis of sarcopenia as the onset may be influenced, but its rate may not.

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